Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: A0A3Q8IH77
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0008612 | peptidyl-lysine modification to peptidyl-hypusine | 3 | 11 |
GO:0009058 | biosynthetic process | 2 | 11 |
GO:0018193 | peptidyl-amino acid modification | 5 | 11 |
GO:0018205 | peptidyl-lysine modification | 6 | 11 |
GO:0019538 | protein metabolic process | 3 | 11 |
GO:0036211 | protein modification process | 4 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043412 | macromolecule modification | 4 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0051604 | protein maturation | 4 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 5 |
GO:0016740 | transferase activity | 2 | 5 |
GO:0016765 | transferase activity, transferring alkyl or aryl (other than methyl) groups | 3 | 5 |
GO:0034038 | deoxyhypusine synthase activity | 4 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 395 | 399 | PF00656 | 0.405 |
CLV_C14_Caspase3-7 | 519 | 523 | PF00656 | 0.330 |
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.415 |
CLV_NRD_NRD_1 | 417 | 419 | PF00675 | 0.806 |
CLV_NRD_NRD_1 | 437 | 439 | PF00675 | 0.468 |
CLV_NRD_NRD_1 | 568 | 570 | PF00675 | 0.572 |
CLV_NRD_NRD_1 | 577 | 579 | PF00675 | 0.763 |
CLV_NRD_NRD_1 | 64 | 66 | PF00675 | 0.449 |
CLV_PCSK_FUR_1 | 152 | 156 | PF00082 | 0.456 |
CLV_PCSK_FUR_1 | 566 | 570 | PF00082 | 0.591 |
CLV_PCSK_FUR_1 | 577 | 581 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 154 | 156 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 193 | 195 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 435 | 437 | PF00082 | 0.689 |
CLV_PCSK_KEX2_1 | 568 | 570 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 577 | 579 | PF00082 | 0.767 |
CLV_PCSK_PC1ET2_1 | 154 | 156 | PF00082 | 0.462 |
CLV_PCSK_PC1ET2_1 | 435 | 437 | PF00082 | 0.689 |
CLV_PCSK_PC1ET2_1 | 579 | 581 | PF00082 | 0.611 |
CLV_PCSK_SKI1_1 | 432 | 436 | PF00082 | 0.779 |
CLV_PCSK_SKI1_1 | 568 | 572 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 79 | 83 | PF00082 | 0.486 |
CLV_Separin_Metazoa | 170 | 174 | PF03568 | 0.533 |
DEG_SPOP_SBC_1 | 440 | 444 | PF00917 | 0.708 |
DOC_CKS1_1 | 406 | 411 | PF01111 | 0.630 |
DOC_CYCLIN_yCln2_LP_2 | 406 | 412 | PF00134 | 0.711 |
DOC_CYCLIN_yCln2_LP_2 | 82 | 85 | PF00134 | 0.402 |
DOC_MAPK_gen_1 | 480 | 486 | PF00069 | 0.337 |
DOC_MAPK_MEF2A_6 | 503 | 512 | PF00069 | 0.169 |
DOC_MAPK_RevD_3 | 555 | 569 | PF00069 | 0.528 |
DOC_PP2B_LxvP_1 | 82 | 85 | PF13499 | 0.402 |
DOC_SPAK_OSR1_1 | 121 | 125 | PF12202 | 0.447 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 428 | 432 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 440 | 444 | PF00917 | 0.784 |
DOC_USP7_MATH_2 | 527 | 533 | PF00917 | 0.330 |
DOC_USP7_UBL2_3 | 435 | 439 | PF12436 | 0.755 |
DOC_WW_Pin1_4 | 302 | 307 | PF00397 | 0.397 |
DOC_WW_Pin1_4 | 390 | 395 | PF00397 | 0.365 |
DOC_WW_Pin1_4 | 405 | 410 | PF00397 | 0.531 |
LIG_14-3-3_CanoR_1 | 173 | 178 | PF00244 | 0.538 |
LIG_14-3-3_CanoR_1 | 193 | 201 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 334 | 341 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 375 | 381 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 568 | 576 | PF00244 | 0.609 |
LIG_14-3-3_CanoR_1 | 577 | 587 | PF00244 | 0.750 |
LIG_Actin_WH2_2 | 269 | 286 | PF00022 | 0.515 |
LIG_APCC_ABBA_1 | 543 | 548 | PF00400 | 0.349 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.469 |
LIG_BIR_III_2 | 573 | 577 | PF00653 | 0.631 |
LIG_BRCT_BRCA1_1 | 261 | 265 | PF00533 | 0.452 |
LIG_BRCT_BRCA1_1 | 392 | 396 | PF00533 | 0.388 |
LIG_deltaCOP1_diTrp_1 | 308 | 316 | PF00928 | 0.434 |
LIG_DLG_GKlike_1 | 173 | 181 | PF00625 | 0.500 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.357 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.568 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.469 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.537 |
LIG_FHA_1 | 480 | 486 | PF00498 | 0.374 |
LIG_FHA_1 | 507 | 513 | PF00498 | 0.374 |
LIG_FHA_2 | 258 | 264 | PF00498 | 0.583 |
LIG_FHA_2 | 303 | 309 | PF00498 | 0.432 |
LIG_GBD_Chelix_1 | 317 | 325 | PF00786 | 0.476 |
LIG_GBD_Chelix_1 | 457 | 465 | PF00786 | 0.429 |
LIG_GBD_Chelix_1 | 55 | 63 | PF00786 | 0.480 |
LIG_HCF-1_HBM_1 | 97 | 100 | PF13415 | 0.434 |
LIG_LIR_Apic_2 | 159 | 164 | PF02991 | 0.640 |
LIG_LIR_Apic_2 | 402 | 407 | PF02991 | 0.561 |
LIG_LIR_Gen_1 | 262 | 273 | PF02991 | 0.404 |
LIG_LIR_Gen_1 | 294 | 304 | PF02991 | 0.509 |
LIG_LIR_Gen_1 | 42 | 50 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 539 | 549 | PF02991 | 0.374 |
LIG_LIR_Gen_1 | 77 | 87 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 262 | 268 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 294 | 299 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 532 | 536 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 539 | 545 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 550 | 555 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 77 | 83 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 97 | 103 | PF02991 | 0.372 |
LIG_LYPXL_S_1 | 99 | 103 | PF13949 | 0.447 |
LIG_LYPXL_yS_3 | 100 | 103 | PF13949 | 0.447 |
LIG_Pex14_2 | 392 | 396 | PF04695 | 0.412 |
LIG_PTB_Apo_2 | 248 | 255 | PF02174 | 0.443 |
LIG_PTB_Phospho_1 | 248 | 254 | PF10480 | 0.446 |
LIG_SH2_CRK | 161 | 165 | PF00017 | 0.635 |
LIG_SH2_PTP2 | 80 | 83 | PF00017 | 0.480 |
LIG_SH2_SRC | 296 | 299 | PF00017 | 0.532 |
LIG_SH2_STAP1 | 204 | 208 | PF00017 | 0.633 |
LIG_SH2_STAT3 | 254 | 257 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.605 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 404 | 407 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 552 | 555 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 80 | 83 | PF00017 | 0.447 |
LIG_SH3_1 | 161 | 167 | PF00018 | 0.633 |
LIG_SH3_3 | 161 | 167 | PF00018 | 0.592 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.490 |
LIG_SH3_3 | 249 | 255 | PF00018 | 0.507 |
LIG_SH3_3 | 450 | 456 | PF00018 | 0.633 |
LIG_SH3_3 | 557 | 563 | PF00018 | 0.423 |
LIG_SH3_3 | 78 | 84 | PF00018 | 0.447 |
LIG_SUMO_SIM_anti_2 | 507 | 513 | PF11976 | 0.169 |
LIG_SUMO_SIM_par_1 | 507 | 513 | PF11976 | 0.246 |
LIG_SUMO_SIM_par_1 | 553 | 559 | PF11976 | 0.444 |
LIG_TRAF2_1 | 167 | 170 | PF00917 | 0.565 |
LIG_TRFH_1 | 80 | 84 | PF08558 | 0.480 |
LIG_UBA3_1 | 149 | 154 | PF00899 | 0.528 |
LIG_WRC_WIRS_1 | 269 | 274 | PF05994 | 0.414 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.576 |
MOD_CK1_1 | 214 | 220 | PF00069 | 0.770 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.544 |
MOD_CK1_1 | 330 | 336 | PF00069 | 0.630 |
MOD_CK1_1 | 390 | 396 | PF00069 | 0.463 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.468 |
MOD_CK1_1 | 441 | 447 | PF00069 | 0.782 |
MOD_CK1_1 | 479 | 485 | PF00069 | 0.330 |
MOD_CK1_1 | 592 | 598 | PF00069 | 0.761 |
MOD_CK2_1 | 257 | 263 | PF00069 | 0.591 |
MOD_CK2_1 | 302 | 308 | PF00069 | 0.440 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.532 |
MOD_GlcNHglycan | 134 | 138 | PF01048 | 0.709 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.652 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.373 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.484 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.705 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.600 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.698 |
MOD_GlcNHglycan | 590 | 594 | PF01048 | 0.695 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.501 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.669 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.657 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.730 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.444 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.587 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.665 |
MOD_GSK3_1 | 442 | 449 | PF00069 | 0.752 |
MOD_GSK3_1 | 506 | 513 | PF00069 | 0.246 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.620 |
MOD_LATS_1 | 417 | 423 | PF00433 | 0.728 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.517 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.346 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.321 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.744 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.476 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.625 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.346 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.353 |
MOD_PIKK_1 | 21 | 27 | PF00454 | 0.564 |
MOD_PK_1 | 419 | 425 | PF00069 | 0.726 |
MOD_PKA_1 | 438 | 444 | PF00069 | 0.674 |
MOD_PKA_1 | 568 | 574 | PF00069 | 0.538 |
MOD_PKA_1 | 578 | 584 | PF00069 | 0.589 |
MOD_PKA_2 | 333 | 339 | PF00069 | 0.560 |
MOD_PKA_2 | 376 | 382 | PF00069 | 0.468 |
MOD_PKA_2 | 568 | 574 | PF00069 | 0.538 |
MOD_PKA_2 | 579 | 585 | PF00069 | 0.580 |
MOD_PKB_1 | 436 | 444 | PF00069 | 0.676 |
MOD_PKB_1 | 566 | 574 | PF00069 | 0.534 |
MOD_Plk_1 | 399 | 405 | PF00069 | 0.475 |
MOD_Plk_1 | 506 | 512 | PF00069 | 0.374 |
MOD_Plk_1 | 547 | 553 | PF00069 | 0.338 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.512 |
MOD_Plk_4 | 376 | 382 | PF00069 | 0.369 |
MOD_Plk_4 | 387 | 393 | PF00069 | 0.361 |
MOD_Plk_4 | 400 | 406 | PF00069 | 0.484 |
MOD_Plk_4 | 506 | 512 | PF00069 | 0.199 |
MOD_Plk_4 | 548 | 554 | PF00069 | 0.334 |
MOD_ProDKin_1 | 302 | 308 | PF00069 | 0.396 |
MOD_ProDKin_1 | 390 | 396 | PF00069 | 0.364 |
MOD_ProDKin_1 | 405 | 411 | PF00069 | 0.544 |
MOD_SUMO_for_1 | 153 | 156 | PF00179 | 0.535 |
MOD_SUMO_for_1 | 525 | 528 | PF00179 | 0.444 |
MOD_SUMO_rev_2 | 431 | 437 | PF00179 | 0.681 |
MOD_SUMO_rev_2 | 86 | 94 | PF00179 | 0.419 |
TRG_DiLeu_BaEn_1 | 6 | 11 | PF01217 | 0.572 |
TRG_DiLeu_BaEn_2 | 117 | 123 | PF01217 | 0.355 |
TRG_DiLeu_BaLyEn_6 | 551 | 556 | PF01217 | 0.330 |
TRG_ENDOCYTIC_2 | 100 | 103 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 296 | 299 | PF00928 | 0.531 |
TRG_ENDOCYTIC_2 | 43 | 46 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 546 | 549 | PF00928 | 0.334 |
TRG_ENDOCYTIC_2 | 552 | 555 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.447 |
TRG_ER_diArg_1 | 192 | 194 | PF00400 | 0.409 |
TRG_ER_diArg_1 | 565 | 568 | PF00400 | 0.546 |
TRG_ER_diArg_1 | 576 | 578 | PF00400 | 0.745 |
TRG_NLS_Bipartite_1 | 418 | 439 | PF00514 | 0.685 |
TRG_NLS_Bipartite_1 | 568 | 582 | PF00514 | 0.563 |
TRG_NLS_MonoExtC_3 | 434 | 439 | PF00514 | 0.684 |
TRG_NLS_MonoExtN_4 | 432 | 439 | PF00514 | 0.690 |
TRG_NLS_MonoExtN_4 | 576 | 582 | PF00514 | 0.599 |
TRG_Pf-PMV_PEXEL_1 | 121 | 125 | PF00026 | 0.335 |
TRG_Pf-PMV_PEXEL_1 | 57 | 61 | PF00026 | 0.448 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HXU4 | Leptomonas seymouri | 54% | 100% |
A0A1X0P8R7 | Trypanosomatidae | 38% | 100% |
A0A422NFI0 | Trypanosoma rangeli | 37% | 100% |
A4HAE7 | Leishmania braziliensis | 76% | 100% |
A4I9K3 | Leishmania infantum | 100% | 100% |
B5APK2 | Leishmania donovani | 99% | 100% |
D0A1W5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9B4K1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q38BX0 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 37% | 100% |
Q4Q3H5 | Leishmania major | 93% | 100% |
V5BRS6 | Trypanosoma cruzi | 38% | 100% |